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SAMD9L-Associated Hereditary Myelodysplastic Syndrome

MedGen UID:
1719321
•Concept ID:
C5239091
•
Neoplastic Process
Synonyms: SAMD9L-Associated Familial MDS; SAMD9L-Associated Familial Myelodysplastic Syndrome

Definition

A familial myelodysplastic syndrome caused by inherited mutations in the SAMD9L gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSAMD9L-Associated Hereditary Myelodysplastic Syndrome

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